Medline recalls specific GYN procedure kits due to a slight dimensional variation that may cause increased difficulty fitting into outer canisters. Affected kits have unique reference numbers and lot codes.
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Medline is recalling certain GYN procedure kits because a small size variation might make them harder to fit into their outer containers. This could lead to handling issues during medical procedures.
The kits have a slight dimensional variation that can cause them to be harder to fit into their outer canisters. This might lead to increased difficulty during medical procedures, but it does not pose a direct safety hazard like injury or fire.
Medical professionals using the recalled kits are most at risk. Patients using these kits during procedures may experience handling difficulties.
Check for reference numbers like DYNJ905499B, DYNJ909936, or DYNJ902371J on the kit labels. Lot numbers such as 23JBI037 or 23KBP829 are also indicators of affected units.
Look for reference numbers like DYNJ905499B, DYNJ909936, or DYNJ902371J on the kit labels.
Medline recalls these kits because a slight dimensional variation may cause increased difficulty fitting into outer canisters during medical procedures.
Check for reference numbers like DYNJ905499B, DYNJ909936, or DYNJ902371J on the kit labels, along with specific lot numbers such as 23JBI037 or 23KBP829.
The recall record does not specify a remedy, so no action is required beyond checking if your kit has the listed reference numbers and lot codes.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2712-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2712-2024 from Medline. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
